A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081720



Internal ID21512632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9352522..9383188hg38UCSC Ensembl
chr12:9505118..9535784hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3830667
hg1930667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665379
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081720
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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